Transcription of Guide to Interpreting Genomic Reports: A Genomics Toolkit
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Guide to Interpreting Genomic Reports: A Genomics Toolkit
Guide to Interpreting Genomic Reports: A Genomics ToolkitA Guide to Genomic test results for non-genetics providersCreated by the Practitioner Education Working Group of the Clinical Sequencing Exploratory Research (CSER) ConsortiumAuthorsKelly East, MS, CGC, Wendy Chung MD, PhD, Kate Foreman, MS, CGC, Mari Gilmore, MS, CGC, Michele Gornick, PhD, Lucia Hindorff, PhD, Tia Kauffman, MPH, Donna Messersmith , PhD, Cindy Prows, MSN, APRN, CNS, Elena Stoffel, MD, Joon-Ho Yu, MPh, PhD and Sharon Plon, MD, PhDAbout this resourceThis resource was created by a team of Genomic testing experts. It is designed to help non-geneticist healthcare providers to understand Genomic medicine and genome sequencing. The CSER Consortium1 is an NIH-funded group exploring Genomic testing in clinical work was conducted as part of the Clinical Sequencing Exploratory Research (CSER) Consortium, grants U01 HG006485, U01 HG006485, U01 HG006546, U01 HG006492, UM1 HG007301, UM1 HG007292, UM1 HG006508, U01 HG006487, U01 HG006507, R01 HG006618, and U01 HG007307.
Genetic Tests vs. Genomic Tests Genetic testing allows for the identification of changes in chromosomes, genes, or proteins (a genes encoded product). The results can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder.
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